Gibbs A, Mackenzie A
Research School of Biological Sciences, Australian National University, Canberra.
J Virol Methods. 1997 Jan;63(1-2):9-16. doi: 10.1016/s0166-0934(96)02103-9.
Sequence analysis was used to design a pair of degenerate oligonucleotide primers that amplified a 1.6-2.1 kbp fragment from the 3' end of the genome (virion protein gene and part of the NIb gene) of 17 species of the Potyviridae ('potyvirids'); 11 potyviruses, 2 bymoviruses, 2 macluraviruses, an ipomovirus and a rymovirus. The 'potyvirid primer 1' hybridizes to the 3' terminal poly-A region of the genome, and 'potyvirid primer 2' to the genomic region encoding the-GNNSGQ-motif of the NIb protein. Database searches showed that the potyvirid 2 primer is specific for potyvirids. Associated analyses indicated that the published amino acid sequence of part of the wheat streak mosaic rymovirus NIb protein is probably incorrect in part.
序列分析用于设计一对简并寡核苷酸引物,该引物从17种马铃薯Y病毒科(“马铃薯Y病毒类病毒”)病毒基因组的3'端(病毒粒子蛋白基因和NIb基因的一部分)扩增出一个1.6 - 2.1 kbp的片段;其中包括11种马铃薯Y病毒、2种大麦黄花叶病毒、2种葛苣花叶病毒、1种甘薯潜隐病毒和1种小麦线条花叶病毒。“马铃薯Y病毒类病毒引物1”与基因组的3'末端多聚A区域杂交,“马铃薯Y病毒类病毒引物2”与编码NIb蛋白-GNNSGQ-基序的基因组区域杂交。数据库搜索表明,马铃薯Y病毒类病毒引物2对马铃薯Y病毒类病毒具有特异性。相关分析表明,已发表的小麦线条花叶病毒NIb蛋白部分氨基酸序列可能部分有误。